The role of ammonia metabolism in nitrogen catabolite repression in Saccharomyces cerevisiae

被引:220
作者
ter Schure, EG
van Riel, NAW
Verrips, CT
机构
[1] Unilever Res Labs Vlaardingen, NL-3133 AT Vlaardingen, Netherlands
[2] Univ Utrecht, Dept Mol Cell Biol, NL-3584 CH Utrecht, Netherlands
关键词
nitrogen metabolism; Saccharomyces cerevisiae; ammonia; catabolite repression; regulation;
D O I
10.1016/S0168-6445(99)00030-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Saccharomyces cerevisiae is able to use a wide variety of nitrogen sources for growth. Not all nitrogen sources support growth equally well. In order to select the best out of a large diversity of available nitrogen sources, the yeast has developed molecular mechanisms. These mechanisms consist of a sensing mechanism and a regulatory mechanism which includes induction of needed systems, and repression of systems that are not beneficial. The first step in use of most nitrogen sources is its uptake via more or less specific permeases. Hence the first level of regulation is encountered at this level. The next step is the degradation of the nitrogen source to useful building blocks via the nitrogen metabolic pathways. These pathways can be divided into routes that lead to the degradation of the nitrogen source to ammonia and glutamate, and routes that lead to the synthesis of nitrogen containing compounds in which glutamate and glutamine are used as nitrogen donor. Glutamine is synthesized out of ammonia and glutamate. The expression of the specific degradation routes is also regulated depending on the availability of a particular nitrogen source. Ammonia plays a central role as intermediate between degradative and biosynthetic pathways. It not only functions as a metabolite in metabolic reactions but is also involved in regulation of metabolic pathways at several levels. This review describes the central role of ammonia in nitrogen metabolism This role is illustrated at the level of enzyme activity, translation and transcription. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:67 / 83
页数:17
相关论文
共 126 条
[31]   EXPRESSION OF THE DAL80 GENE, WHOSE PRODUCT IS HOMOLOGOUS TO THE GATA FACTORS AND IS A NEGATIVE REGULATOR OF MULTIPLE NITROGEN CATABOLIC GENES IN SACCHAROMYCES-CEREVISIAE, IS SENSITIVE TO NITROGEN CATABOLITE REPRESSION [J].
CUNNINGHAM, TS ;
COOPER, TG .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6205-6215
[32]   THE SACCHAROMYCES-CEREVISIAE DAL80 REPRESSOR PROTEIN BINDS TO MULTIPLE COPIES OF GATAA-CONTAINING SEQUENCES (URS(GATA)) [J].
CUNNINGHAM, TS ;
COOPER, TG .
JOURNAL OF BACTERIOLOGY, 1993, 175 (18) :5851-5861
[33]   THE UGA4 UAS(NTR) SITE REQUIRED FOR GLN3-DEPENDENT TRANSCRIPTIONAL ACTIVATION ALSO MEDIATES DAL80-RESPONSIVE REGULATION AND DAL80 PROTEIN-BINDING IN SACCHAROMYCES-CEREVISIAE [J].
CUNNINGHAM, TS ;
DORRINGTON, RA ;
COOPER, TG .
JOURNAL OF BACTERIOLOGY, 1994, 176 (15) :4718-4725
[34]   The CCAAT box-binding factor stimulates ammonium assimilation in Saccharomyces cerevisiae, defining a new cross-pathway regulation between nitrogen and carbon metabolisms [J].
Dang, VD ;
Bohn, C ;
BolotinFukuhara, M ;
DaignanFornier, B .
JOURNAL OF BACTERIOLOGY, 1996, 178 (07) :1842-1849
[35]   REGULATORY CIRCUIT FOR RESPONSES OF NITROGEN CATABOLIC GENE-EXPRESSION TO THE GLN3-PROTEIN AND DAL80-PROTEIN AND NITROGEN CATABOLITE REPRESSION IN SACCHAROMYCES-CEREVISIAE [J].
DAUGHERTY, JR ;
RAI, R ;
ELBERRY, HM ;
COOPER, TG .
JOURNAL OF BACTERIOLOGY, 1993, 175 (01) :64-73
[36]   PHOSPHORYLATION OF INITIATION FACTOR-2-ALPHA BY PROTEIN-KINASE GCN2 MEDIATES GENE-SPECIFIC TRANSLATIONAL CONTROL OF GCN4 IN YEAST [J].
DEVER, TE ;
FENG, L ;
WEK, RC ;
CIGAN, AM ;
DONAHUE, TF ;
HINNEBUSCH, AG .
CELL, 1992, 68 (03) :585-596
[37]   Integration of the multiple controls regulating the expression of the arginase gene CAR1 of Saccharomyces cerevisiae in response to different nitrogen signals: Role of Gln3p, ArgRp-Mcm1p, and Ume6p [J].
Dubois, E ;
Messenguy, F .
MOLECULAR & GENERAL GENETICS, 1997, 253 (05) :568-580
[38]  
Filetici P, 1996, YEAST, V12, P1359, DOI 10.1002/(SICI)1097-0061(199610)12:13<1359::AID-YEA3>3.0.CO
[39]  
2-5
[40]   IDENTIFICATION AND CHARACTERIZATION OF HAP4 - A 3RD COMPONENT OF THE CCAAT-BOUND HAP2 HAP3 HETEROMER [J].
FORSBURG, SL ;
GUARENTE, L .
GENES & DEVELOPMENT, 1989, 3 (08) :1166-1178